All terms in MONDO
| Label | Id | Description |
|---|---|---|
| 46,XX true hermaphroditism, SRY-positive | MONDO_0800381 | |
| 46,XX disorder of sex development | MONDO_0017576 | |
| Joubert syndrome 11 | MONDO_0800382 | |
| eosinophil peroxidase deficiency | MONDO_0043364 | |
| cerebrospinal fluid leak | MONDO_0043327 | |
| cardioacrofacial dysplasia | MONDO_0031386 | |
| autoinflammatory syndrome, familial, Behcet-like | MONDO_0031384 | |
| hereditary disorder of connective tissue | MONDO_0023603 | |
| Mirizzi syndrome | MONDO_0043330 | |
| extrahepatic cholestasis | MONDO_0006757 | |
| lathyrism | MONDO_0043339 | |
| congenital disorder of deglycosylation | MONDO_0031376 | |
| progressive transformation of germinal centers | MONDO_0043346 | |
| lymphoma | MONDO_0005062 | |
| Chilaiditi syndrome | MONDO_0043343 | |
| colonic disorder | MONDO_0003409 | |
| odontochondrodysplasia | MONDO_0031169 | |
| spondylometaphyseal dysplasia | MONDO_0016763 | |
| macular dystrophy, retinal | MONDO_0031166 | |
| genetic macular dystrophy | MONDO_0020242 |